ライフサイエンスコーパス: feline immunodeficiency virus

1 y virus, equine infectious anemia virus, and feline immunodeficiency virus.

2 been obtained from animals infected with the feline immunodeficiency virus.

3 us, human immunodeficiency virus type 1, and feline immunodeficiency virus.

4 his model can also explain 3TC resistance in feline immunodeficiency virus and human hepatitis B viru

5 Frameshifting pseudoknots in feline immunodeficiency virus and simian retrovirus have

6 ly inhibit replication of human, simian, and feline immunodeficiency viruses and therefore has broad-

7 the dominant selective force acting on this feline immunodeficiency virus as it replicates in a new

8 To address these issues, we used a feline immunodeficiency virus-based (FIV-based) vector.

9 d into the articular joint space a defective feline immunodeficiency virus capable of infecting divid

10 ne was prepared from a pathogenic isolate of feline immunodeficiency virus containing a mutation that

11 s, we evaluated the molecular evolution of a feline immunodeficiency virus derived from a wild cougar

12 ion, delivery of this shRNA by a recombinant feline immunodeficiency virus effectively silenced torsi

13 tant role that CXCR4 plays in infection with feline immunodeficiency virus, expression on PBMC in viv

14 ction with the prototypic Petaluma strain of feline immunodeficiency virus (FIV(PET)) using vaccines

15 GFAP-IL-1betaXAT mice were injected with the feline immunodeficiency virus (FIV) (Cre) vector in the

16 The feline immunodeficiency virus (FIV) accessory factor, Or

17 The neurotoxic effects of the feline immunodeficiency virus (FIV) and FIV envelope pro

18 To determine its antiviral activity against feline immunodeficiency virus (FIV) and HIV, the activit

19 Feline immunodeficiency virus (FIV) and human immunodefi

20 ThX and mock-ThX cats were inoculated with feline immunodeficiency virus (FIV) and monitored for th

21 The surface glycoprotein (gp95) of the feline immunodeficiency virus (FIV) binds in a strain-sp

22 an immunodeficiency virus type 2 (HIV-2) and feline immunodeficiency virus (FIV) but not HIV-1.

23 semen from male domestic cats infected with feline immunodeficiency virus (FIV) can transmit virus t

24 Feline immunodeficiency virus (FIV) causes AIDS-like sym

25 Infection with feline immunodeficiency virus (FIV) causes an immunosupp

26 Feline immunodeficiency virus (FIV) causes progressive i

27 The process of feline immunodeficiency virus (FIV) cell entry was exami

28 We have identified feline immunodeficiency virus (FIV) clinical isolates th

29 6-residue multiepitopic synthetic peptide of feline immunodeficiency virus (FIV) comprising immunodom

30 tested the hypothesis that vectors based on feline immunodeficiency virus (FIV) could be used for co

31 Feline immunodeficiency virus (FIV) does not infect huma

32 combinant soluble CD134 (sCD134) facilitated feline immunodeficiency virus (FIV) entry into CXCR4-pos

33 A heterologous feline immunodeficiency virus (FIV) expression system pe

34 (n = 19) had been chronically infected with feline immunodeficiency virus (FIV) for over 6 years, wh

35 We previously observed feline immunodeficiency virus (FIV) Gag accumulating at

36 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) had different patter

37 Feline immunodeficiency virus (FIV) induces a disease st

38 Similar to human immunodeficiency virus, feline immunodeficiency virus (FIV) induces immunodefici

39 In feline immunodeficiency virus (FIV) infected cats, daily

40 Feline immunodeficiency virus (FIV) infection in cats pr

41 s during the acute stage (first 4 months) of feline immunodeficiency virus (FIV) infection in laborat

42 Feline immunodeficiency virus (FIV) infection in the cat

43 A monoclonal antibody, MAb vpg15, inhibits feline immunodeficiency virus (FIV) infection in tissue

44 The acute stage of feline immunodeficiency virus (FIV) infection is charact

45 The acute stage of feline immunodeficiency virus (FIV) infection is charact

46 Disease progression of feline immunodeficiency virus (FIV) infection is charact

47 vestigating the effect of CCR5 expression on feline immunodeficiency virus (FIV) infection must be in

48 cells (Tregs) activated during the course of feline immunodeficiency virus (FIV) infection suppress C

49 Herein we demonstrate that in vitro feline immunodeficiency virus (FIV) infection, but not U

50 rly target cells and tissues in transmucosal feline immunodeficiency virus (FIV) infection, cats were

51 viral replication during the acute stage of feline immunodeficiency virus (FIV) infection.

52 Feline immunodeficiency virus (FIV) infects many species

53 Feline immunodeficiency virus (FIV) infects numerous wil

54 Feline immunodeficiency virus (FIV) is a lentivirus of d

55 Feline immunodeficiency virus (FIV) is a lentivirus that

56 Feline immunodeficiency virus (FIV) is a lentivirus that

57 Feline immunodeficiency virus (FIV) is a lentivirus that

58 Feline immunodeficiency virus (FIV) is a lentivirus whic

59 The orf-A (orf-2) gene of feline immunodeficiency virus (FIV) is a small open read

60 Feline immunodeficiency virus (FIV) is among the most co

61 evelopment of gene delivery vectors based on feline immunodeficiency virus (FIV) is an attractive alt

62 Infection of domestic cats with feline immunodeficiency virus (FIV) is an important mode

63 ogenetic distance from primate lentiviruses, feline immunodeficiency virus (FIV) is becoming the lent

64 of equine infectious anemia virus (EIAV) and feline immunodeficiency virus (FIV) is inhibited by lept

65 The disease induced in cats by feline immunodeficiency virus (FIV) is similar to HIV in

66 Feline immunodeficiency virus (FIV) is similar to human

67 Feline immunodeficiency virus (FIV) is the feline analog

68 ptional elements within the U3 domain of the feline immunodeficiency virus (FIV) long terminal repeat

69 Using the feline immunodeficiency virus (FIV) model of HIV we eval

70 The feline immunodeficiency virus (FIV) model of vertical hu

71 By using the feline immunodeficiency virus (FIV) model, we have docum

72 Previous studies using feline immunodeficiency virus (FIV) molecular clones lac

73 Feline immunodeficiency virus (FIV) naturally infects mu

74 candidates were tested for activity against feline immunodeficiency virus (FIV) on infected CrFK cel

75 Feline immunodeficiency virus (FIV) OrfA is an accessory

76 were evaluated for their incorporation onto feline immunodeficiency virus (FIV) particles, transduct

77 We have used feline immunodeficiency virus (FIV) protease (PR) as a m

78 We used feline immunodeficiency virus (FIV) protease (PR) as a m

79 A novel fluorogenic substrate for continuous feline immunodeficiency virus (FIV) protease (PR) assay

80 The feline immunodeficiency virus (FIV) protease is essentia

81 Feline immunodeficiency virus (FIV) protease is structur

82 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) proteases (PRs).

83 The presence of feline immunodeficiency virus (FIV) proviral DNA, expres

84 A feline immunodeficiency virus (FIV) provirus with a vif

85 ilar to human immunodeficiency virus type 1, feline immunodeficiency virus (FIV) replicates in the th

86 ron (IFN-alpha) induced tetherin and blocked feline immunodeficiency virus (FIV) replication in lymph

87 regulatory properties and ability to support feline immunodeficiency virus (FIV) replication in vitro

88 Mutants of feline immunodeficiency virus (FIV) resistant to (-)-bet

89 Intravaginal inoculation of cats with feline immunodeficiency virus (FIV) results in acute sys

90 ily conserved on both HIV type 1 (HIV-1) and feline immunodeficiency virus (FIV) reverse transcriptas

91 The structure of the putative feline immunodeficiency virus (FIV) ribosomal frameshift

92 We had previously demonstrated that feline immunodeficiency virus (FIV) RNA levels in plasma

93 Feline immunodeficiency virus (FIV) shares with T-cell t

94 The major surface glycoprotein of feline immunodeficiency virus (FIV) specifically binds t

95 A cytopathic variant of feline immunodeficiency virus (FIV) strain PPR emerged a

96 The feline immunodeficiency virus (FIV) targets activated CD

97 t syncytium formation mediated by strains of feline immunodeficiency virus (FIV) that have been selec

98 immunodeficiency virus (HIV) and strains of feline immunodeficiency virus (FIV) that have been selec

99 Variants of feline immunodeficiency virus (FIV) that possess a uniqu

100 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) the least.

101 We compared feline immunodeficiency virus (FIV) to other restricted

102 ssion in arthritic joints of mice, using the feline immunodeficiency virus (FIV) vector, which is cap

103 The ability of feline immunodeficiency virus (FIV) vectors to transfer

104 V), bovine immunodeficiency virus (BIV), and feline immunodeficiency virus (FIV) Vif appear specific

105 Stable expression of feline immunodeficiency virus (FIV) Vif-green fluorescen

106 Vertical transmission of feline immunodeficiency virus (FIV) was studied in cats

107 y RNA ligands for reverse transcriptase from feline immunodeficiency virus (FIV) were isolated from a

108 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) were prepared to exa

109 binant Vif derived from the 34TF10 strain of feline immunodeficiency virus (FIV) were used to assess

110 we generated a defective mutant provirus of feline immunodeficiency virus (FIV) with an in-frame del

111 Feline immunodeficiency virus (FIV), a lentivirus, cause

112 d from the pathogenic GL8 molecular clone of feline immunodeficiency virus (FIV), a range of viral va

113 xamined the brains of cats infected with the feline immunodeficiency virus (FIV), an animal model of

114 human immunodeficiency virus type 1 (HIV-1), feline immunodeficiency virus (FIV), and equine infectio

115 l leukemia virus type 1 (HTLV-1), HIV-1, and feline immunodeficiency virus (FIV), and have been postu

116 Human immunodeficiency virus type 1 (HIV-1), feline immunodeficiency virus (FIV), and Moloney murine

117 BIV), equine infectious anemia virus (EIAV), feline immunodeficiency virus (FIV), and Rous sarcoma vi

118 cells and cell lines did not restrict HIV-1, feline immunodeficiency virus (FIV), equine infectious a

119 Feline immunodeficiency virus (FIV), like other members

120 of CD134 is the primary binding receptor for feline immunodeficiency virus (FIV), targeting the virus

121 (fCD134) is the primary binding receptor for feline immunodeficiency virus (FIV), targeting the virus

122 f human acquired immune deficiency syndrome, feline immunodeficiency virus (FIV), was used to model m

123 For the rapid genetic analysis of feline immunodeficiency virus (FIV), we developed a hete

124 Feline immunodeficiency virus (FIV)-based lentiviral vec

125 natural lung tropism; however, pseudotyping feline immunodeficiency virus (FIV)-based lentiviral vec

126 r efficiency and tissue or cell tropism of a feline immunodeficiency virus (FIV)-based lentiviral vec

127 pression following a single application of a feline immunodeficiency virus (FIV)-based lentivirus vec

128 epatoma cells following gene transfer with a feline immunodeficiency virus (FIV)-based lentivirus vec

129 arget these apical receptors, we pseudotyped feline immunodeficiency virus (FIV)-based vectors by usi

130 When recombinant feline immunodeficiency virus (FIV)-based vectors expres

131 We investigated the efficacy of feline immunodeficiency virus (FIV)-based vectors in tar

132 gical signals' alterations, we have used the feline immunodeficiency virus (FIV)-derived gp120 and ev

133 influence of the protease inhibitor TL-3 on feline immunodeficiency virus (FIV)-induced central nerv

134 We analyzed antibody responses in sera from feline immunodeficiency virus (FIV)-infected and uninfec

135 and immunodeficiency is a characteristic of feline immunodeficiency virus (FIV)-infected cats, it is

136 s were mucosally challenged with 10(2)-10(6) feline immunodeficiency virus (FIV)-infected T cells.

137 lymphocytes that suppress the replication of feline immunodeficiency virus (FIV).

138 ferent cell tropisms for molecular clones of feline immunodeficiency virus (FIV).

139 ld cat following experimental infection with feline immunodeficiency virus (FIV).

140 of viral mRNAs produced in cells infected by feline immunodeficiency virus (FIV).

141 es in the production of infectious HIV-1 and feline immunodeficiency virus (FIV).

142 f many viruses, including strains of HIV and feline immunodeficiency virus (FIV).

143 ell line protect cats against challenge with feline immunodeficiency virus (FIV).

144 suppresses the infectivity of vif-defective feline immunodeficiency virus (FIV).

145 nonuclear cell (PBMC) subsets in response to feline immunodeficiency virus (FIV).

146 The feline immunodeficiency virus (FIV)/cat system was used

147 An infectious chimeric feline immunodeficiency virus (FIV)/HIV strain carrying

148 immunity to infection can be induced against feline immunodeficiency virus (FIV); however, protection

149 ase (IN) mutants for a non-human lentivirus (feline immunodeficiency virus [FIV]) and analyzed both t

150 Feline lentiviral (feline immunodeficiency virus [FIV]) encapsidation has n

151 onprimate lentiviral genomic RNAs (HIV-1 and feline immunodeficiency virus [FIV]) vis-a-vis their Gag

152 , we demonstrate that a fast-evolving virus (feline immunodeficiency virus, FIV) can reveal details o

153 transmission pathways for three subtypes of feline immunodeficiency virus (FIVPle ) in African lions

154 DGF/p75-dependent disparity was observed for feline immunodeficiency virus IN.

155 tranasal insulin treatment of experimentally feline immunodeficiency virus-infected animals resulted

156 This investigation of feline immunodeficiency virus infection in bobcats and p

157 IDS, and their homologues may play a role in feline immunodeficiency virus infection.

158 s of MLV integrase and truncated variants of feline immunodeficiency virus integrase, suggesting that

159 (HIV-2), simian immunodeficiency virus, and feline immunodeficiency virus integrases.

160 ian immunodeficiency virus, puma lentivirus, feline immunodeficiency virus, Jembrana disease virus, v

161 The earliest experiments were in the cat/feline immunodeficiency virus model, followed a decade l

162 A full-length feline immunodeficiency virus NCSU1 (FIV-NCSU1) genome (

163 Lion lentivirus (LLV; also known as feline immunodeficiency virus of lion, Panthera leo [FIV

164 d with feline lentiviruses (puma lentivirus, feline immunodeficiency virus Pco [FIV-Pco], referred to

165 structures of complexes of a D30N mutant of feline immunodeficiency virus protease (FIV PR) complexe

166 is a protease inhibitor developed using the feline immunodeficiency virus protease as a model.

167 es in success when targeting HIV-1 protease, feline immunodeficiency virus protease, and HIV-1 integr

168 S3' subsite binding specificities of HIV and feline immunodeficiency virus proteases (FIV) proteases

169 l cross-species transmission of a subtype of feline immunodeficiency virus, puma lentivirus A (PLVA),

170 TRIMCyp transgenic cat lymphocytes resisted feline immunodeficiency virus replication.

171 e similarities to the export signal found in feline immunodeficiency virus Rev protein.

172 of cells productively infected with HIV-1 or feline immunodeficiency virus revealed dramatic patterns

173 nus of tRNA(Lys,3) and the U5-IR loop of the feline immunodeficiency virus RNA genome suggests a nove

174 Except for the feline immunodeficiency virus, sequences similar to the

175 of HIV, infection of neonatal cats with the feline immunodeficiency virus, showed development of per

176 enetic diversity, and molecular evolution of feline immunodeficiency virus specific to cougars (FIVpc

177 used to compare the nucleotide sequences of feline immunodeficiency virus strains isolated from Texa

178 eported previously for functional binding of feline immunodeficiency virus SU to its coreceptor CD134

179 zed a highly pathogenic molecular isolate of feline immunodeficiency virus subtype C (FIV-C) CABCpady

180 of cellular receptors for human, simian, and feline immunodeficiency viruses that are tropic for lymp

181 Finally, replacing nucleotides of the feline immunodeficiency virus U5-IR loop with the (A)(4)

182 A feline immunodeficiency virus vector encoding both full-

183 , we report that human DC-SIGN also captures feline immunodeficiency virus via high-affinity (1 nM),

184 CV-N potently blocked infection by feline immunodeficiency virus, which utilizes the chemok